Reply To: MY DAD HAS ACUTE GBS/NOT WAKING UP, IS NOT ON SEDATION MEDS

I was diagnosed with MFS back in 2004, at that time no one said anything about there being any kind of cranium paralyzation. My MFS lasted about 8 or 9 months before I was back to normal. 10 years later I now have nerve pain that the doctors seen to think is from the MFS. Now this pain has caused me to become unable to work because of all the meds for pain I have to take. I hope things work out for you.